Key result
Endothelial progenitor cell therapy significantly reduced the elevated expression levels of various atherosclerosis-associated microRNAs in plasma, platelets, and platelet-derived microvesicles in a hypertensive-hyperlipidemic hamster model.
Why the study?
The study aimed to analyze miRNA expression profiles in plasma, platelets, and platelet-derived microvesicles in experimental atherosclerosis and investigate the effect of endothelial progenitor cell transplantation.
Does endothelial progenitor cell therapy improve microRNA expression profiles in plasma, platelets, and platelet-derived microvesicles in a hypertensive-hyperlipidemic hamster model?
Does endothelial progenitor cell therapy improve microRNA expression profiles in plasma, platelets, and platelet-derived microvesicles in a hypertensive-hyperlipidemic hamster model?
EPC therapy reverses the pro-atherogenic microRNA expression profiles in plasma, platelets, and microvesicles induced by hypertension and hyperlipidemia in a preclinical model.
EPC miRNA effects remain preclinical; hypothesis-generating and should not yet alter patient management.
The aim of this study was to analyze the expressed profiles of miRNAs in plasma, platelets and platelet-derived microvesicles (PMVs) obtained from experimental induced atherosclerosis animal model and to investigate the effect of EPC transplantation on these profiles. Methods. Seventeen selected circulating miRNAs (miR-19a,-21,-126,-146a,-223,-26b,-92a,-222,-210,-221, -143,-10a,-145,-155,-34a,-204, and miR-214) were individually analyzed in plasma, platelets and PMVs isolated from peripheral blood of hypertensive-hyperlipidemic hamsters treated or not with endothelial progenitor cells (EPCs), and of healthy hamsters taken as control group. Results. Comparative with control group, in hypertension associated with hyperlipidemia the investigated miRNA expression profiles were different: (i) in plasma, the levels of all investigated miRNAs were significantly increased, the highest enhances being noticed for miR-21,-146a,-221,-143,-34a and miR-204; (ii) in platelets, the expressions of almost all miRNAs were significantly elevated, remarkable for miR-126,-146a,-223,-222 and miR-214, while levels of miR-143, miR-10a, and miR-145 were significantly reduced; (iii) in PMVs, numerous miRNAs were found to have significantly increased levels, especially miR-222,-221,-210 and miR-34a, whereas expressions of various miRNAs as miR-223,-214,-146a,-143,-10a and miR-145 were significantly decreased. The treatment with EPCs had the following reverse effects: (i) in plasma, significantly reduced the expression of miR-26b,-143,-34a,-204 and miR-214; (ii) in platelets, significantly decreased the levels of almost investigated miRNAs, with remarkably diminishing for miR-126 and miR-221; and (iii) in PMVs, significantly lowered the expression of some miRNAs, with considerably reductions for miR-222, -221, -210 and miR-19a, while the level of miR-214 was found elevated. Conclusions. The present study revealed that miRNAs have differential expression profiles in plasma, platelets and PMVs under hypertension associated with hyperlipidemia conditions. The different miRNA profile in PMVs compared with platelets indicated an active mechanism of selective packing of miRNAs into PMVs from maternal cells; various miRNAs such as miR-19a,-21,-126,-26b,-92a,-155,-204,-210,-221,-222 and -34a delivered by PMVs may contribute to enrichment of circulating plasma miRNA expression. In addition, our study showed that the EPC-based therapy can regulate the expressions of investigated miRNAs into the three sources. These results provide novel information that could help in finding potential targets for the development of new therapeutic strategies in the cardiovascular disease.
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Alexandru et al. (2019) studied Hypertension associated with hyperlipidemia (n=30). Endothelial progenitor cell (EPC) therapy vs. Hypertensive-hyperlipidemic diet without EPC therapy was evaluated on Expression profiles of 17 selected circulating miRNAs in plasma, platelets, and PMVs (p=≤0.05). Endothelial progenitor cell therapy significantly reduced the elevated expression levels of various atherosclerosis-associated microRNAs in plasma, platelets, and platelet-derived microvesicles in a hypertensive-hyperlipidemic hamster model.
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